Canonical Allele Identifier: CA2427968761

Gene: ARAF

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566807G= , CM000685.2:g.47566807G=	GRCh38
NC_000023.10:g.47426206G= , CM000685.1:g.47426206G=	GRCh37
NC_000023.9:g.47311150G=	NCBI36
NG_016339.1:g.10691G=
NG_016339.2:g.10691G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.699+27G= MANE Select	ENSP00000366244.4:n.699+27G=
ENST00000290277.10:c.708+27G=	ENSP00000290277.7:n.708+27G=
ENST00000377045.8:c.699+27G=	ENSP00000366244.4:n.699+27G=
NM_001256196.1:c.708+27G=	NP_001243125.1:n.708+27G=
NM_001654.4:c.699+27G=	NP_001645.1:n.699+27G=
XM_006724529.1:c.714+27G=	XP_006724592.1:n.714+27G=
XM_011543906.1:c.714+27G=	XP_011542208.1:n.714+27G=
XM_011543907.1:c.714+27G=	XP_011542209.1:n.714+27G=
XM_011543908.1:c.699+27G=	XP_011542210.1:n.699+27G=
XM_011543909.1:c.42+27G=	XP_011542211.1:n.42+27G=
XM_006724529.3:c.714+27G=	XP_006724592.1:n.714+27G=
XM_011543906.3:c.714+27G=	XP_011542208.1:n.714+27G=
XM_011543908.3:c.699+27G=	XP_011542210.1:n.699+27G=
XM_011543909.3:c.42+27G=	XP_011542211.1:n.42+27G=
NM_001654.5:c.699+27G= MANE Select	NP_001645.1:n.699+27G=
NM_001256196.2:c.708+27G=	NP_001243125.1:n.708+27G=